Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1378995Erstellt: 26. Oktober 2026

Methyl iodide → (E)-8-(3-Bromostyryl)-1,3-diethyl-7-methylxanthine (6d)

https://huagongshe.com/reaction/1378995

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktPotassium CarbonateHCID 11430—
Edukt1H-Purine-2,6-dione, 3,7-dihydro-8-(2-(3-bromophenyl)ethenyl)-1,3-diethyl-, (E)-HCID 6448930—
LösungsmittelDimethylformamideHCID 6228—
Produkt(E)-8-(3-Bromostyryl)-1,3-diethyl-7-methylxanthine (6d)HCID 6448931—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

Compound g (2.5 g, 6.43 mmol) obtained in Reference Example 7 was dissolved in 20 ml of dimethylformamide. To the solution were added 2.22 g (16.1 mmol) of potassium carbonate and subsequently 0.8 ml (12.9 mmol) of methyl iodide, and the resulting mixture was stirred at 50° C. for 70 minutes. After cooling, insoluble matters were filtered off and water was added to the filtrate. The mixture was extracted three times with chloroform. The extract was washed three times with water and subsequently twice with a saturated aqueous solution of sodium chloride, and dried over anhydrous sodium sulfate. Evaporation under reduced pressure gave 2.37 g (yield 92%) of crude Compound h as a yellow solid, which was further recrystallized from cyctohexane/toluene to give Compound h as a yellow powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05670498
Quelldatensatzuspto-grants-1997_09
ORD IDord-40e6c0c6eb144d9aae726f345076b4ae
Quellennotizuspto-grants-1997_09